Label: GLYREG (aceticum acidum, cacao, magnesia sulphurica, natrum sulphuricum, verbascum thapsus, glandula suprarenalis suis, pancreas suis, cortisone aceticum, thyroidinum- suis, iodium, lycopodium clavatum, phosphorus, ranunculus bulbosus, saccharum officinale, vanadium metallicum, zincum metallicum, chromium acidum, culex musca liquid
- NDC Code(s): 43742-1931-1
- Packager: Deseret Biologicals, Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated April 23, 2024
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ACTIVE INGREDIENTS:
Aceticum Acidum 3X, 6, 12X, 30X, Cacao 6X, Chromium Acidum 16X, Cortisone Aceticum 8X, 12X, 30X, Culex Musca 16X, Glandula Suprarenalis Suis 8X, Iodium 12X, Lycopodium Clavatum 12X, Magnesia Sulphurica 6X, Natrum Sulphuricum 6X, Pancreas Suis 8X, Phosphorus 12X, Ranunculus Bulbosus 12X, Saccharum Officinale 12X, Thyroidinum (Suis) 8X, 12X, 30X, Vanadium Metallicum 12X, Verbascum Thapsus 6X, Zincum Metallicum 12X.
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PURPOSE:
Aceticum Acidum - Hunger, Cacao – Self Induced Vertigo, Chromium Acidum – Brain Fog, Cortisone Aceticum - Hunger, Culex Musca – Brain Fog, Glandula Suprarenalis Suis - Fatigue, Iodium - Shakiness, Lycopodium Clavatum - Cravings, Magnesia Sulphurica - Irritability, Natrum Sulphuricum - Fatigue, Pancreas Suis - Hunger, Phosphorus – Self Induced Vertigo, Ranunculus Bulbosus – Brain Fog, Saccharum Officinale - Shakiness, Thyroidinum (Suis) - Fatigue, Vanadium Metallicum - Cravings, Verbascum Thapsus - Irritability, Zincum Metallicum – Brain Fog
- USES:
- WARNINGS:
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- INACTIVE INGREDIENTS:
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INGREDIENTS AND APPEARANCE
GLYREG
aceticum acidum, cacao, magnesia sulphurica, natrum sulphuricum, verbascum thapsus, glandula suprarenalis suis, pancreas suis, cortisone aceticum, thyroidinum (suis), iodium, lycopodium clavatum, phosphorus, ranunculus bulbosus, saccharum officinale, vanadium metallicum, zincum metallicum, chromium acidum, culex musca liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-1931 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETIC ACID (UNII: Q40Q9N063P) (ACETIC ACID - UNII:Q40Q9N063P) ACETIC ACID 3 [hp_X] in 1 mL COCOA (UNII: D9108TZ9KG) (COCOA - UNII:D9108TZ9KG) COCOA 6 [hp_X] in 1 mL MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE 6 [hp_X] in 1 mL SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 6 [hp_X] in 1 mL VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172) (VERBASCUM THAPSUS - UNII:C9TD27U172) VERBASCUM THAPSUS WHOLE 6 [hp_X] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 8 [hp_X] in 1 mL SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS 8 [hp_X] in 1 mL CORTISONE ACETATE (UNII: 883WKN7W8X) (CORTISONE - UNII:V27W9254FZ) CORTISONE ACETATE 8 [hp_X] in 1 mL THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) THYROID 8 [hp_X] in 1 mL IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 12 [hp_X] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS WHOLE 12 [hp_X] in 1 mL SUCROSE (UNII: C151H8M554) (SUCROSE - UNII:C151H8M554) SUCROSE 12 [hp_X] in 1 mL VANADIUM (UNII: 00J9J9XKDE) (VANADIUM - UNII:00J9J9XKDE) VANADIUM 12 [hp_X] in 1 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 12 [hp_X] in 1 mL CHROMIUM TRIOXIDE (UNII: 8LV49809UC) (CHROMIUM TRIOXIDE - UNII:8LV49809UC) CHROMIUM TRIOXIDE 16 [hp_X] in 1 mL CULEX PIPIENS (UNII: 45KA5D7541) (CULEX PIPIENS - UNII:45KA5D7541) CULEX PIPIENS 16 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-1931-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 10/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/26/2020 Labeler - Deseret Biologicals, Inc (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-1931) , api manufacture(43742-1931) , label(43742-1931) , pack(43742-1931)